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The Manager, Revenue Accounting is responsible for management of Group Purchasing Organizations (GPO) and distributor pricing relationships and collections of account receivables; related internal controls and ensure that reported results comply with generally accepted accounting principles.
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Dendreon is seeking a dedicated Medical Science Liaison to join its Medical Affairs team. This person will have the opportunity to work with the only approved immune-oncology therapy for prostate cancer. Successful candidates will master clinical information on sipuleucel-T and speak to the immunologic basis for its therapeutic effect. This individual will serve as a resource to healthcare professionals caring for prostate cancer patients, facilitate the successful implementation of clinical trials, and provide field perspective to Dendreon. The territory alignment for this role is: : CT, MA, ME, NH, NJ, NY, PA, MD, DC, DE, RI, and VT.
The preferred residing area for this territory is fairly close in airport proximity of the greater New York City area, Boston or Philadelphia.
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Dendreon’s Immunotherapy Sales Specialist is responsible for achieving sales objectives in an assigned territory through the development, maintenance, and enhancement of the business. Customers include oncologists, urologists, nurses, pharmacists, pharmacy and therapeutics groups, tumor boards, teaching institutions, hospitals and formulary committees. The role is responsible for ensuring customer’s clinical conviction in the product as well as guiding the customer through the logistics process and seeing the sale through to its conclusion. The territory alignment for this role is: central east of midstate south, not including Fort Myers and west.
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Dendreon Technical Operations manages the creation of the production plan and execution of arm-to-arm activities supporting Provenge treatments, including but not limited to production and demand planning, logistics analysis, scheduling, and real-time product monitoring.
The Customer Order Specialist is responsible for processing the receipt of Dendreon enrollment forms, managing order information, responding to inquiries, and triaging issues for resolution according to organization and operational objectives. The ideal candidate is someone with data management skills willing to work in a dynamic and fast-paced customer service environment. Ability to manage customer relationships and communicate with internal teams is important to be successful in this role. An eye for detail and ability to understand how operational systems work is highly recommended.
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The Director, Enterprise Applications is responsible for managing the Enterprise Applications team and outsourced managed service providers that have specific responsibility for acquiring, building or configuring, maintaining or enhancing, supporting, and eventually decommissioning enterprise business applications and databases through their life cycle. Dendreon’s enterprise business applications include ERP and its family of supporting products and a complement of proprietary in-house applications. The role establishes and maintains policies, procedures, and governance as it relates to the company’s application portfolio. The Director, Enterprise Applications is responsible for providing oversight, implementing appropriate controls and performing regular and effective reviews of all technical aspects, including DevOps activities.
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The Supervisor, Manufacturing will report to the Manufacturing Operations Manager and is responsible for overseeing the planning and monitoring of manufacturing process activities and works closely with plant personnel to ensure the execution of production activities per the master treatment schedule.
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Dendreon is seeking a dedicated Medical Science Liaison to join its Medical Affairs team. This person will have the opportunity to work with the only approved immune-oncology therapy for prostate cancer. Successful candidates will master clinical information on sipuleucel-T and speak to the immunologic basis for its therapeutic effect. This individual will serve as a resource to healthcare professionals caring for prostate cancer patients, facilitate the successful implementation of clinical trials, and provide field perspective to Dendreon. The territory alignment for this role: IA,IL,IN, KY, MI, ND, NE, OH, SD, WI.
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The Sr. Quality Specialist, Maufacturing Quality is responsible for performing a wide variety of QA activities to ensure compliance with applicable regulatory requirements.
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The Supervisor, Quality Control, Microbiology is responsible for the providing daily supervision of lab operations (people, process, product) for one or more functional areas within Quality Control. Ensures the site, process, product, and personnel are compliant with regulatory requirements.
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The Manager, Bioassay is responsible for the oversight, planning, coordination, and supervision of technical and operational activities in the Bioassay laboratory.
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The Corporate Account Manager responsible for the execution within community-based key focus accounts designated by the A-B-C-D targeting methodology. The CAM approaches each customer with a total account management perspective by leveraging all available and approved resources appropriately. They collaborate with business partners (within and outside the company) to accurately and compliantly articulate the PROVENGE value proposition to their customers. The alignment for this territory are the following states: Alaska, Washington, Montana, Idaho, Oregon, Nevada, and Utah.
Ideal candidate will reside in the following states close to a major airport: Washington, Oregon or Boise.
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Dendreon Pharmaceuticals seeks a Director, Supplier Quality at the Seal Beach, CA site. The Director, Supplier Quality position is responsible and accountable for the execution of all Dendreon activities associated with the full Supplier Quality function, covering both GMP and GTP suppliers, to ensure patient safety. The role ensures the site, process, product, and personnel are compliant with all applicable regulatory requirements. It will be a key partner to all Executive Quality and Operations Leadership to ensure FDA readiness. This role is a key strategic quality leader and needs substantial experience in GMP operations, GTP operations, regulatory inspections, internal and external audit, and excellent verbal and written communication skills.
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The Quality Analyst I, Bioassay is responsible for performing daily lab operations with the assigned functional area related to the release of product, and/or monitoring of the IMF environment, as well as complete other assigned duties.
Shift for this role is Sunday: 5:00PM-5:00AM Monday and Tuesday: 9:30PM-9:30AM
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The Director/Sr Director of Regulatory Affairs is responsible for leading and/or participating on interdisciplinary regulatory teams responsible for defining and implementing regulatory strategy, including plans to submit Marketing Applications globally. Provides regulatory leadership on cross-functional development teams.
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Dendreon is seeking a Director for Medical Affairs Communications and Intelligence (MACI) to provide strategic and operational direction for the development and execution of field and medical affairs communications and competitive intelligence in support of the clinical immunotherapy and HEOR initiatives with Dendreon Pharmaceuticals, LLC.
The successful candidate will lead the Medical Affairs Communications and Intelligence function, and develop and execute the strategies relevant to medical communications for sipuleucel-T. These activities will include, but are not limited to, the development of scientific and medical communication resources such as slide decks, clinical/scientific FAQs, literature surveillance, and competitive intelligence collections. The role will have a key part in the organization and scientific content development for Dendreon at major scientific congresses, medical meetings, and advisory boards. The Director for MACI works closely with Corporate Communications and Training department as well as other cross-functional partners, including Medical Information, PV, Publications, HEOR, V.P. of Medical Affairs, and Clinical Development to inform and execute the medical communication strategies. The position will require a strong understanding and interpretation of the clinical, economic, and humanistic data collected and generated to support sipuleucel-T and future development compounds.
The successful candidate should have excellent communication and presentation skills, and a record of accomplishSavement working in a cross-functional collaborative environment. He or she should have a background in the life sciences industry with experience in translating clinical data into clear, concise evidence and communication plans for both payer and clinical audiences in both academia and community practice.
Flexibility to work from a remote location or onsite in the Seattle office.
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Targeting Cancer, Transforming Lives At Dendreon, patients come first. We are one team, acting together, with a shared purpose of improving patients' lives through science. If you are passionate about the fight against cancer and looking for a career in an exciting, cutting-edge field, you may be a perfect fit for our team.
This position is the heart and soul of our organization. You will be responsible for the manufacturing of the PROVENGE® (sipuleucel-T) product in a clean-room environment. The product is manufactured using our patients’ blood.
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Dendreon is seeking a dedicated Medical Science Liaison to join its Medical Affairs team. This person will have the opportunity to work with the only approved immune-oncology therapy for prostate cancer. Successful candidates will master clinical information on sipuleucel-T and speak to the immunologic basis for its therapeutic effect. This individual will serve as a resource to healthcare professionals caring for prostate cancer patients, facilitate the successful implementation of clinical trials, and provide field perspective to Dendreon.
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The Sr. Quality Specialist, Computer Systems Validation individual is responsible for providing Quality & Compliance oversight to ensure compliance with Computer System Validation (CSV), Systems Development Lifecycle (SDLC) and Data Integrity.
